Scott syndrome (Q7437571)

From Wikidata
Jump to: navigation, search
inherited blood coagulation disease characterized by autosomal recessive inheritance of hemorrhagic episodes due to impaired platelet coagulant activity that has material basis in homozygous mutation in the TMEM16F gene on chromosome 12q12
  • familial prothrombin consumption inhibitor
  • familial prothrombin conversion defect
  • prothrombin consumption deficiency
  • bleeding abnormality due to deficiency of platelet biding of factor X
  • BDPLT7
  • platelet-type bleeding disorder 7
  • SCTS
edit
Language Label Description Also known as
English
Scott syndrome
inherited blood coagulation disease characterized by autosomal recessive inheritance of hemorrhagic episodes due to impaired platelet coagulant activity that has material basis in homozygous mutation in the TMEM16F gene on chromosome 12q12
  • familial prothrombin consumption inhibitor
  • familial prothrombin conversion defect
  • prothrombin consumption deficiency
  • bleeding abnormality due to deficiency of platelet biding of factor X
  • BDPLT7
  • platelet-type bleeding disorder 7
  • SCTS

Statements

Identifiers

 
edit
edit
    edit
      edit
        edit
          edit
            edit
              edit
                edit